Canonical Allele Identifier: CA347484847
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551869C>A , CM000664.2:g.85551869C>A GRCh38
NC_000002.11:g.85778992C>A , CM000664.1:g.85778992C>A GRCh37
NC_000002.10:g.85632503C>A NCBI36
NG_011811.2:g.14666G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.6030G>T
ENST00000482662.2:n.4437G>T
ENST00000685865.1:n.2389G>T
ENST00000687250.1:n.2089G>T
ENST00000687995.1:n.1904G>T
ENST00000688205.1:c.*1145G>T ENSP00000509673.1:n.*1145G>T
ENST00000688788.1:n.1791G>T
ENST00000689276.1:c.1483G>T ENSP00000510012.1:p.Glu495Ter
ENST00000689576.1:c.*171G>T ENSP00000508712.1:n.*171G>T
ENST00000690108.1:c.*1208G>T ENSP00000510617.1:n.*1208G>T
ENST00000690468.1:c.*104G>T ENSP00000509078.1:n.*104G>T
ENST00000690595.1:c.877G>T ENSP00000508979.1:p.Glu293Ter
ENST00000691348.1:c.*104G>T ENSP00000509369.1:n.*104G>T
ENST00000691410.1:c.*1129G>T ENSP00000508479.1:n.*1129G>T
ENST00000693287.1:c.868G>T ENSP00000510264.1:p.Glu290Ter
ENST00000693681.1:c.865G>T ENSP00000510789.1:p.Glu289Ter
ENST00000233838.9:c.1552G>T MANE Select ENSP00000233838.3:p.Glu518Ter
ENST00000233838.8:c.1552G>T ENSP00000233838.3:p.Glu518Ter
ENST00000430215.7:c.1381G>T ENSP00000408045.3:p.Glu461Ter
ENST00000465637.5:n.179-3865G>T
NM_000821.5:c.1552G>T NP_000812.2:p.Glu518Ter
NM_000821.6:c.1552G>T NP_000812.2:p.Glu518Ter
NM_001142269.2:c.1381G>T NP_001135741.1:p.Glu461Ter
NM_001142269.3:c.1381G>T NP_001135741.1:p.Glu461Ter
XM_005264259.3:c.1552G>T XP_005264316.1:p.Glu518Ter
XM_011532764.1:c.730G>T XP_011531066.1:p.Glu244Ter
XM_011532765.1:c.730G>T XP_011531067.1:p.Glu244Ter
XR_939677.1:n.1465G>T
XM_005264259.5:c.1552G>T XP_005264316.1:p.Glu518Ter
XM_011532764.3:c.730G>T XP_011531066.1:p.Glu244Ter
XM_011532765.3:c.730G>T XP_011531067.1:p.Glu244Ter
XM_017003803.2:c.1381G>T XP_016859292.1:p.Glu461Ter
XR_001738703.2:n.1465G>T
NM_000821.7:c.1552G>T MANE Select NP_000812.2:p.Glu518Ter
NM_001142269.4:c.1381G>T NP_001135741.1:p.Glu461Ter